Guest guest Posted November 18, 2008 Report Share Posted November 18, 2008 Hello- I am curious to hear from anyone taking LDN? I have RRMS for 4 years now, only took Copaxone for 6 months in the beginning. Looking for alternatives... Thanks in advance. Carolyn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2008 Report Share Posted November 18, 2008 Hi Carolyn, You can find a number of LDN-related testimonials at http://tinyurl.com/intro-to-ldn For additional information about treating MS, visit http://tinyurl.com/advice-to-msers Sincerely, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2008 Report Share Posted November 18, 2008 Thanks for the Info. I just called my neuro and he said he would write a prescription when I go in on Monday... Thanks again- Carolyn Subject: Re: LDN To: mscured Date: Tuesday, November 18, 2008, 1:40 PM Hi Carolyn, You can find a number of LDN-related testimonials at http://tinyurl. com/intro- to-ldn For additional information about treating MS, visit http://tinyurl. com/advice- to-msers Sincerely, Dudley Delany http://profiles. yahoo.com/ dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2009 Report Share Posted May 6, 2009 Hi Vicki, For information about LDN and other promising alternative MS treatment options, visit http://tinyurl.com/advice-to-msers With best wishes, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2009 Report Share Posted May 24, 2009 Hi , I had a similar experience with LDN. My legs hurt and they were stiff. I stopped taking it and I have not gotten worse. I wasn't walking when I started it. I'm still not walking but many of the symptoms that I had are no longer issues. Fatigue and brain fog are gone and I'm not in atrophy anymore. I don't have footdrop, I don't have incontenence. LDN may not work for everyone but it's worth trying. It might work. It has helped many people. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2009 Report Share Posted June 23, 2009 Hi , Welcome to the group! Here is a website you may find helpful in treating your MS: http://tinyurl.com/advice-to-msers It includes important information about LDN. With best wishes, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2009 Report Share Posted August 12, 2009 Hi Pam, For information about LDN and other promising options in the treatment of MS, visit http://tinyurl.com/advice-to-msers Honey feeds Candida yeast. I think you would be better off using Stevia. With best wishes, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2009 Report Share Posted August 12, 2009 Another question I went from drinking white wine to red and I didn't feel so good today, now when I make my slds with old and red wine vinegar my legs hurt is there something that might be in the both of them, any thoughts would be great. ________________________________ To: mscured Sent: Wednesday, August 12, 2009 5:16:31 PM Subject: Re: LDN Hi Pam, For information about LDN and other promising options in the treatment of MS, visit http://tinyurl. com/advice- to-msers Honey feeds Candida yeast. I think you would be better off using Stevia. With best wishes, Dudley Delany http://profiles. yahoo.com/ dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 13, 2009 Report Share Posted August 13, 2009 Ditch the chips. Fried food is to be avoided as it is loaded with trans fat. You need to be on a strict Best Bet Diet--no cheating!!! There are some good links (including a video clip) regarding the BBD at http://tinyurl.com/advice-to-msers Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 13, 2009 Report Share Posted August 13, 2009 Hello Pam, The mscured site forwards the messages to my email, so i hope you don;t mind my responding in this way. My name is Roxann, and i was diagnosed with primary progressive ms. I live in England, and i am on LDN. Are you in England too, cos if you are, i can tell you how to get it here. If you want to know about the LDN, type: googleldn.com it is a site hosted by ph wouk and he will tell you everything you want to know about it. The site even tells you how to get it in America. TTFN, Roxy Subject: LDN To: mscured Date: Wednesday, 12 August, 2009, 8:15 PM what is it? what does it do for you? how do I get it? Just started Best Bet Diet....had a meltdown last night and ate 1/2 a carton of chocolte ice cream....ugh! !! I got into poison ivy really bad and had to start predesone... .makes me really anxious so I got the ice cream out!! I think I will miss the dessert I love so much at night. I did change to honey for my tea...is that ok? Pam PS I would love to have some MS chat friends...I love to garden, have my dogs, I am lesbian and like to read...I am home all week alone and would love to chat with other women/men that want to talk about the MS but other things too. Pam Quote Link to comment Share on other sites More sharing options...
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